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靶向髓过氧化物酶(MPO)介导的氧化应激和炎症以减轻脑缺血损伤:天然化合物的潜在应用

Targeting Myeloperoxidase (MPO) Mediated Oxidative Stress and Inflammation for Reducing Brain Ischemia Injury: Potential Application of Natural Compounds.

作者信息

Chen Shuang, Chen Hansen, Du Qiaohui, Shen Jiangang

机构信息

School of Chinese Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.

Shenzhen Institute of Research and Innovation, The University of Hong Kong, Shenzhen, China.

出版信息

Front Physiol. 2020 May 19;11:433. doi: 10.3389/fphys.2020.00433. eCollection 2020.

Abstract

Oxidative stress and inflammation are two critical pathological processes of cerebral ischemia-reperfusion injury. Myeloperoxidase (MPO) is a critical inflammatory enzyme and therapeutic target triggering both oxidative stress and neuroinflammation in the pathological process of cerebral ischemia-reperfusion injury. MPO is presented in infiltrated neutrophils, activated microglial cells, neurons, and astrocytes in the ischemic brain. Activation of MPO can catalyze the reaction of chloride and HO to produce HOCl. MPO also mediates oxidative stress by promoting the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS), modulating the polarization and inflammation-related signaling pathways in microglia and neutrophils. MPO can be a therapeutic target for attenuating oxidative damage and neuroinflammation in ischemic stroke. Targeting MPO with inhibitors or gene deficiency significantly reduced brain infarction and improved neurological outcomes. This article discusses the important roles of MPO in mediating oxidative stress and neuroinflammation during cerebral ischemia-reperfusion injury and reviews the current understanding of the underlying mechanisms. Furthermore, we summarize the active compounds from medicinal herbs with potential as MPO inhibitors for anti-oxidative stress and anti-inflammation to attenuate cerebral ischemia-reperfusion injury, and as adjunct therapeutic agents for extending the window of thrombolytic treatment. We highlight that targeting MPO could be a promising strategy for alleviating ischemic brain injury, which merits further translational study.

摘要

氧化应激和炎症是脑缺血再灌注损伤的两个关键病理过程。髓过氧化物酶(MPO)是一种关键的炎症酶和治疗靶点,在脑缺血再灌注损伤的病理过程中引发氧化应激和神经炎症。MPO存在于缺血脑内浸润的中性粒细胞、活化的小胶质细胞、神经元和星形胶质细胞中。MPO的激活可催化氯离子与HO反应生成HOCl。MPO还通过促进活性氧(ROS)和活性氮(RNS)的产生、调节小胶质细胞和中性粒细胞的极化及炎症相关信号通路来介导氧化应激。MPO可以作为减轻缺血性卒中氧化损伤和神经炎症的治疗靶点。用抑制剂或基因缺陷靶向MPO可显著减少脑梗死并改善神经功能结局。本文讨论了MPO在脑缺血再灌注损伤期间介导氧化应激和神经炎症中的重要作用,并综述了对其潜在机制的当前认识。此外,我们总结了具有作为MPO抑制剂潜力的药用植物活性化合物,用于抗氧化应激和抗炎以减轻脑缺血再灌注损伤,并作为辅助治疗剂以延长溶栓治疗的时间窗。我们强调靶向MPO可能是减轻缺血性脑损伤的一种有前景的策略,值得进一步的转化研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e459/7248223/e65f8928addd/fphys-11-00433-g001.jpg

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